A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811318



Internal ID21256656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:24574744..24574744hg38UCSC Ensembl
chr5:24574853..24574853hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg38985
hg19985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13699867
Samples
Known GenesCDH10
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811318
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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